反应 #355734

ord-380b56030e494935b169924ff1029747

反应方程式

Cc1cc([N+](=O)[O-])ccc1F
4-fluoro-3-methyl nitrobenzene
NCCNCCO
2-(2-aminoethylamino)ethanol
O=C([O-])[O-].[K+].[K+]
K2CO3
CN1CCCC1=O
N-methylpyrrolidinone
Cc1cc([N+](=O)[O-])ccc1NCCNCCO
2-[2-(4-nitro-2-methylphenylamino)ethylamino]ethanol
收率 77.8%

溶剂

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度after cooling to room temperature
  2. 2
    其他The yellow precipitate formed
  3. 3
    过滤was filtered off
  4. 4
    干燥dried over P2O5

实验过程

2 g of 4-fluoro-3-methyl nitrobenzene, 1.61 g of 2-(2-aminoethylamino)ethanol and 2.14 g of K2CO3 were added to a solution of 20 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 7 hours and, after cooling to room temperature, was then poured into a water and ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 2.4 g of 2-[2-(4-nitro-2-methylphenylamino)ethylamino]ethanol (5) were obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07445645B2uspto-grants-2008_11